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Research Topic : Death Signalling
Field of Research : Reproduction
Status : Closed
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Reproduction (21)
Cell Development, Proliferation and Death (4)
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  • Researchers (7)
  • Funded Activities (21)
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  • Funded Activity

    Hedgehog Signalling In Spermatogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $523,842.00
    Summary
    Male fertility requires sufficient production of healthy sperm in the testis. We discovered that cells in the adult testis communicate via the Hedgehog (Hh) signalling pathway as sperm develop. We propose to use a highly specific drug to inhibit Hh activity in order to delineate the precise steps in sperm production affected by Hh signalling. We will study the importance Hh in maintenance of spermatogonial stem cells and create mouse models to learn how it is controlled.
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    Funded Activity

    Understanding Epigenetic Modification During Oogenesis For Novel Treatments Of Female Infertility

    Funder
    National Health and Medical Research Council
    Funding Amount
    $314,644.00
    Summary
    Infertility affects about 10% of Australian women and the success rates of current infertility treatments are low due to our poor knowledge of eggs development. The numbers of obese and older women trying to conceive are increasing; fertility treatments are even less effective for them. I have generated mouse models to elucidate the pathways regulating egg development. I will study for alterations in these pathways in the mouse models which perfectly mimic the obesity and aging in women.
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    Funded Activity

    Developmental Switches In Spermatogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $705,501.00
    Summary
    I seek the knowledge required to improve prevention, diagnosis and therapy for men with testicular pathologies by studying what controls early sperm development. My research will delineate how cellular signalling molecules lay the foundation for adult fertility, using animal studies, cell culture and clinical samples. Testis samples from testicular cancer patients will be used to test interventions that may kill tumour cells or offer a therapeutic option to men with impaired spermatogenesis.
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    Funded Activity

    Uncoupled Research Fellowship

    Funder
    National Health and Medical Research Council
    Funding Amount
    $765,000.00
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    Funded Activity

    Activin And Androgen Crosstalk During Testis Development Programs Adult Fertility

    Funder
    National Health and Medical Research Council
    Funding Amount
    $700,740.00
    Summary
    Fertility in men is determined by how the testis grows during fetal and juvenile life. We recently discovered that the Sertoli cells which nurse developing sperm are highly sensitive to cross-talk between testosterone and the growth factor activin during puberty. This project studies how this cross-talk is controlled to understand how altered hormone actions in boys, including exposure to harmful endocrine disrupting chemicals, reduces adult fertility.
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    Funded Activity

    Manipulating Ovarian Follicle - Oocyte Communication To Control Reproductive Outcomes

    Funder
    National Health and Medical Research Council
    Funding Amount
    $567,424.00
    Summary
    Ovarian follicles provide the environment supporting oocyte (egg) development. Communication between cells of the follicle and oocytes modulate this environment. We discovered new cell surface molecules that receive the signals from the oocyte and we identified a class of drug compounds that can modulate this signalling. This discovery offers a unique potential to therapeutically intervene in this signalling process and both improve infertility therapies and develop new non-steroidal contracepti .... Ovarian follicles provide the environment supporting oocyte (egg) development. Communication between cells of the follicle and oocytes modulate this environment. We discovered new cell surface molecules that receive the signals from the oocyte and we identified a class of drug compounds that can modulate this signalling. This discovery offers a unique potential to therapeutically intervene in this signalling process and both improve infertility therapies and develop new non-steroidal contraceptives.
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    Funded Activity

    Translating Oocyte Biology Discoveries To New Clinical Practices

    Funder
    National Health and Medical Research Council
    Funding Amount
    $772,605.00
    Summary
    A/Professor Gilchrist is a reproductive biologist studying factors that regulate the intrinsic quality of unfertilised eggs. He has produced and patented the use of unique growth factors produced by the egg that enhance egg quality in women. Bringing together industry and a world-leading clinic, he is developing new forms of hormone-free infertility treatment which he will take to clinical practice over the next 5 years.
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    Funded Activity

    The Impact Of Wnt Signaling On Spermatogenesis

    Funder
    National Health and Medical Research Council
    Funding Amount
    $578,352.00
    Summary
    Male fertility requires sufficient production of healthy sperm in the testis. This project builds on our discovery that testicular cells communicate via the wnt family of proteins during sperm development, and that interruption of their activities reduces fertility in mice. We propose to use mouse models to study the precise steps in sperm production affected by Wnt signalling and how it works.
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    Funded Activity

    Discovery Projects - Grant ID: DP160100647

    Funder
    Australian Research Council
    Funding Amount
    $398,000.00
    Summary
    A novel microtubule severing protein involved in male germ cell biology. The project aims to better understand the cellular and biochemical mechanisms underlying a key component of male fertility. Microtubules are a fundamental component of all cells. A mechanism that is increasingly recognised as essential for microtubules regulation is severing. It has been discovered that an uncharacterised microtubule severing protein, KATNAL2, has a key role in male germ cell development. This project aims .... A novel microtubule severing protein involved in male germ cell biology. The project aims to better understand the cellular and biochemical mechanisms underlying a key component of male fertility. Microtubules are a fundamental component of all cells. A mechanism that is increasingly recognised as essential for microtubules regulation is severing. It has been discovered that an uncharacterised microtubule severing protein, KATNAL2, has a key role in male germ cell development. This project aims to define the mechanisms underlying KATNAL2 function in the male germ line. It is expected that these data will generate a comprehensive picture of KATNAL2 function and provide foundation data of relevance across multiple species and tissues. In the longer term, it may also reveal a rational strategy for fertility enhancement or suppression.
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    Funded Activity

    EGF Peptide Signalling Improves Oocyte Maturation And Quality

    Funder
    National Health and Medical Research Council
    Funding Amount
    $586,891.00
    Summary
    Infertility is common and although IVF is widely accepted, the procedure is expensive and is associated with health risks. Using laboratory animals, we have developed significant new insights into mechanisms regulating egg quality. These insights have allowed us to develop a new approach to infertility treatment - crucially, one that eliminates the need for ovarian hormone therapy used in IVF. This project will investigate the basic mechanisms underlying our new approach to enable safe clinical .... Infertility is common and although IVF is widely accepted, the procedure is expensive and is associated with health risks. Using laboratory animals, we have developed significant new insights into mechanisms regulating egg quality. These insights have allowed us to develop a new approach to infertility treatment - crucially, one that eliminates the need for ovarian hormone therapy used in IVF. This project will investigate the basic mechanisms underlying our new approach to enable safe clinical implementation.
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    Showing 1-10 of 21 Funded Activites

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